Evidence map›Paper›PMID 17175356›Full record

ArticleTransplantation proceedings2006

Blood gene expression profiling in liver transplant recipients with hepatitis C virus and posttransplantation diabetes mellitus.

C J Driscoll, A K Cashion, D K Hathaway, C Thompson, Y Conley, C Riely, L Xu, R Homayouni

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In one paragraph

Article in Transplantation proceedings, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 38% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 8 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

C J DriscollCollege of Nursing, University of Tennessee Health Science Center, Memphis, Tennessee, USA. cdrisco2@utmem.edu
A K Cashion
D K Hathaway
C Thompson
Y Conley
C Riely
L Xu
R Homayouni
University of Tennessee Health Science Center · USUniversity of Memphis · USUniversity of Pittsburgh · US

Funding

Gene Expression Profiles of Liver Transplant RecipientsF31NR008650 · NINR · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI DRISCOLL, CAROLYN J · 2004 to 2004
$37k
NINR NIH HHS 1 F31 NR08650-01A1NINR NIH HHS F31 NR008650NINR NIH HHS F31 NR008650-01A1
6 · The paper itself

Abstract

backgroundHepatitis C virus (HCV) is a risk factor for developing posttransplantation diabetes mellitus (PTDM) after liver transplantation; little is known about the biological mechanisms involved with this risk. This study investigated gene expression differences to provide insight into potential mechanisms. PATIENTS AND

methodsGene expression profiles of blood samples obtained from 6 HCV+ liver transplant recipients were determined using Affymetrix U133 Plus 2.0 microarrays. Differential gene expression was assessed between HCV+ recipients with PTDM (n = 3) and without PTDM (n = 3) using the GeneSpring 7.3 software package. The Welch t test was used to identify significant differences (P < .05) between groups. Gene expression profiles for 6 HCV- liver transplant recipients (with PTDM = 3, without PTDM = 3) were used as a blind test set to evaluate a subset of genes to predict PTDM.

resultsExpression levels of 347 genes were significantly different between recipients with PTDM and those without PTDM. Seventy-four genes were up-regulated and 270 were down-regulated in PTDM. Genes were categorized into functional classes: apoptosis (n = 69 genes); immune function (n = 110); diabetes (n = 17); hepatitis C (n = 12); liver transplant (n = 69). The expression profile of a subset of genes was evaluated for predicting PTDM in 6 HCV- transplant recipients. We accurately predicted the presence or absence of PTDM in 5/6 recipients.

conclusionsPTDM in HCV+ liver transplant recipients was associated with down-regulated expression of a large number of genes. A subset of these genes was useful to predict PTDM in HCV- recipients. Most genes were associated with apoptosis and immune function. HCV may act as a primer by affecting a group of genes involved in developing diabetes.

Indexed as

Gene Expression ProfilingBody Mass IndexDiabetes MellitusFemaleGene Expression RegulationHepatitis CHumansLiver TransplantationMaleOligonucleotide Array Sequence AnalysisPostoperative ComplicationsRNARNA

Identifiers

PMID17175356
PMCPMC1847576
OpenAlexW1985851957

What OpenQuestion holds

Textmetadata
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.